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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872126Generated: November 1, 2026

Tetrahydrofuran → Compound 10

https://huagongshe.com/reaction/1872126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium ThiosulfateHCID 24477—
ReactantMethyl morpholine oxideHCID 82029—
Reactanttert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylateHCID 5148195—
CatalystOsmium TetroxideHCID 30318—
ProductCompound 10HCID 13329883—

Reaction Steps

A solution of crude 2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester (10.5 g, 62.1 mmol) in tetrahydro-furan (300 ml) was treated sequentially with osmium tetroxide (2.5 % in t-butanol, 6 mL) and N-methylmorpholine-N-oxide at 25° C. After 48 hours, aqueous 10% sodium thiosulfate solution was added and the mixture was stirred 30 minutes, partially concentrated to remove tetrahydro-furan, and the resulting aqueous mixture extracted twice with ether. The ether extracts were washed with 10% sodium thiosulfate, 0.1N HCl, dried and concentrated giving a dark orange oil which was chromatographed on silica eluted with 1%, 2%, 4%, 8% and 10% ethanol-dichloromethane giving an amber syrup (4.09 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107329
Source datasetuspto-grants-2000_08
ORD IDord-9e41b0db2b554dd99e44413e2f1078e8
Source noteuspto-grants-2000_08